Spodoptera frugiperda is a globally significant migratory agricultural pest that requires proactive monitoring. Understanding the molecular mechanisms underlying the interactions between pathogenic microorganisms and S. frugiperda is crucial for enhancing the effectiveness of microbial control agents against this pest. This study used transcriptome sequencing and molecular biology techniques on S. frugiperda larvae infected by bacteria and fungi to investigate the composition and molecular regulatory mechanisms of its immune system. A total of 598 immune-related genes were identified. Upon microbial infection, most immune-related genes showed an upregulated expression trend. Phylogenetic analysis revealed that the immune gene repertoire of S. frugiperda is relatively conserved. The expression of the genes of peptidoglycan recognition proteins in different tissues of S. frugiperda induced by microorganisms at different times was verified using qPCR, and the results confirmed that these genes were significantly upregulated under specific pathogenic infections. This study elucidates the immune transcriptome of S. frugiperda in response to various pathogenic microorganisms, providing valuable insights for improving the effectiveness of existing microbial agents and developing new, highly efficient, and specific biopesticides.

This study explores the molecular mechanisms underlying diapause in the parasitoid wasp Telenomus remus (Nixon) (Hymenoptera: Platygastridae), a critical egg parasitoid for the biological control of the invasive pest Spodoptera frugiperda (Smith) (Lepidoptera: Noctuidae). While effective in pest management, T. remus faces limitations in large-scale applications due to its short lifespan and low viability under storage conditions. Diapause, a state of developmental arrest, was successfully induced in T. remus using photoperiod manipulation (0L:24D), allowing for extended survival and improved storage potential. Transcriptome sequencing identified 2642 differentially expressed genes, with 617 involved in 284 enriched pathways, including calcium signaling and phototransduction. The study found that the expression levels of CBP1 and CBP2, genes encoding calcium-binding proteins, were significantly downregulated during diapause. As key regulators in calcium ion-mediated signal transduction pathways, the downregulation of CBP1 and CBP2 may lead to the suppression of intracellular calcium signaling, thereby affecting light signal transduction and energy metabolism regulation. This suggests that during diapause, insects may reduce calcium signaling activity to suppress physiological functions, maintain a low metabolic state, and decrease sensitivity to environmental stimuli. Additionally, ARR genes still exhibited differential expression, further supporting their potential role in phototransduction and diapause regulation.

Spodoptera frugiperda is a globally significant migratory agricultural pest that requires proactive monitoring. Understanding the molecular mechanisms underlying the interactions between pathogenic microorganisms and S. frugiperda is crucial for enhancing the effectiveness of microbial control agents against this pest. This study used transcriptome sequencing and molecular biology techniques on S. frugiperda larvae infected by bacteria and fungi to investigate the composition and molecular regulatory mechanisms of its immune system. A total of 655 immune-related genes were identified, including pattern recognition receptors, signal transduction factors, immune effectors, and immune regulators. Following microbial infection, most immune-related genes showed an upregulated expression trend. Phylogenetic analysis revealed that the immune gene repertoire of S. frugiperda is relatively conserved. The expression changes of immune recognition receptors PGRP and βGRP were validated using qPCR, confirming that these genes were significantly upregulated under specific pathogenic infections. This study elucidates the immune transcriptome of S. frugiperda in response to various pathogenic microorganisms, providing valuable insights for improving the effectiveness of existing microbial agents and developing new highly efficient and specific biopesticides.